CRISPR Gene editing therapy is used for the first time in living humans with amazing results.

Scientists say they have used the gene-editing tool CRISPR to repair a person's eyesight for the first time. DNA is short for ...

A newly discovered bacterial defense protein named Cat1 reveals an extraordinary method of viral neutralization. All living ...

Japanese researchers have successfully eliminated the extra chromosome responsible for Down syndrome using CRISPR gene ...

A team at Kobe University has created a game-changing resource for autism research: 63 mouse embryonic stem cell lines, each ...

RNA gene scissors (CRISPR-Cas13) are gaining significant attention as a next-generation gene therapy with fewer side effects.

Researchers have created a standardized mouse stem cell library containing 63 genetic variants strongly linked to autism ...

New research reveals that Gαi3 is overexpressed in bladder cancer and promotes tumour growth via the Akt-mTOR pathway, highlighting its potential as a therapeutic target.

Delve into what the new CRISPR tool, CAST, has to offer. CRISPR-associated transposases are already gaining traction in ...